CA2857192C - Vernis de surimpression a base de dispersions non aqueuses - Google Patents
Vernis de surimpression a base de dispersions non aqueuses Download PDFInfo
- Publication number
- CA2857192C CA2857192C CA2857192A CA2857192A CA2857192C CA 2857192 C CA2857192 C CA 2857192C CA 2857192 A CA2857192 A CA 2857192A CA 2857192 A CA2857192 A CA 2857192A CA 2857192 C CA2857192 C CA 2857192C
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- CA
- Canada
- Prior art keywords
- overprint varnish
- substrate
- acrylic
- aqueous dispersion
- shell polymer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Links
- 239000002966 varnish Substances 0.000 title claims abstract description 183
- 239000006185 dispersion Substances 0.000 title claims abstract description 63
- 229920000642 polymer Polymers 0.000 claims abstract description 215
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 185
- 239000000203 mixture Substances 0.000 claims abstract description 174
- 239000000758 substrate Substances 0.000 claims abstract description 120
- 239000002245 particle Substances 0.000 claims abstract description 77
- 238000000576 coating method Methods 0.000 claims abstract description 47
- 238000000034 method Methods 0.000 claims abstract description 47
- 239000011248 coating agent Substances 0.000 claims abstract description 46
- 238000004383 yellowing Methods 0.000 claims abstract description 40
- 239000003125 aqueous solvent Substances 0.000 claims abstract description 33
- 239000000178 monomer Substances 0.000 claims description 67
- 238000000518 rheometry Methods 0.000 claims description 55
- 239000002904 solvent Substances 0.000 claims description 51
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 44
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 39
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 29
- 229920005989 resin Polymers 0.000 claims description 23
- 239000011347 resin Substances 0.000 claims description 23
- 229930195733 hydrocarbon Natural products 0.000 claims description 20
- 239000004215 Carbon black (E152) Substances 0.000 claims description 17
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 12
- 125000000524 functional group Chemical group 0.000 claims description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 11
- 230000032683 aging Effects 0.000 claims description 11
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 11
- 239000011593 sulfur Substances 0.000 claims description 11
- 229910052717 sulfur Inorganic materials 0.000 claims description 11
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 11
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 10
- 239000003513 alkali Substances 0.000 claims description 10
- 150000001412 amines Chemical class 0.000 claims description 10
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 claims description 10
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 8
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 claims description 8
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 claims description 8
- 230000008569 process Effects 0.000 claims description 8
- 229920001577 copolymer Polymers 0.000 claims description 7
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 6
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 5
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 5
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 5
- 239000011976 maleic acid Substances 0.000 claims description 5
- 229910000000 metal hydroxide Inorganic materials 0.000 claims description 5
- 150000004692 metal hydroxides Chemical class 0.000 claims description 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 5
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 4
- 150000003141 primary amines Chemical class 0.000 claims description 3
- 150000003335 secondary amines Chemical class 0.000 claims description 3
- 150000003512 tertiary amines Chemical class 0.000 claims description 3
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 2
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 claims description 2
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 claims 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims 1
- 150000003973 alkyl amines Chemical class 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 239000002480 mineral oil Substances 0.000 abstract description 8
- 235000010446 mineral oil Nutrition 0.000 abstract description 5
- 238000006243 chemical reaction Methods 0.000 description 59
- 239000000976 ink Substances 0.000 description 47
- 239000011541 reaction mixture Substances 0.000 description 44
- 239000003054 catalyst Substances 0.000 description 40
- 239000012071 phase Substances 0.000 description 33
- 239000000049 pigment Substances 0.000 description 27
- 150000002430 hydrocarbons Chemical class 0.000 description 24
- -1 2-hydroxy ethyl acrylates Chemical class 0.000 description 20
- 239000003505 polymerization initiator Substances 0.000 description 17
- 230000015572 biosynthetic process Effects 0.000 description 16
- 239000003921 oil Substances 0.000 description 16
- 235000019198 oils Nutrition 0.000 description 16
- 230000000052 comparative effect Effects 0.000 description 15
- 239000004615 ingredient Substances 0.000 description 14
- 238000001035 drying Methods 0.000 description 13
- 238000012360 testing method Methods 0.000 description 13
- 238000005259 measurement Methods 0.000 description 12
- 229960004592 isopropanol Drugs 0.000 description 11
- 150000001451 organic peroxides Chemical class 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 9
- 238000003786 synthesis reaction Methods 0.000 description 9
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 9
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 8
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 8
- 239000003999 initiator Substances 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- 239000011356 non-aqueous organic solvent Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 8
- QEQBMZQFDDDTPN-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy benzenecarboperoxoate Chemical compound CC(C)(C)OOOC(=O)C1=CC=CC=C1 QEQBMZQFDDDTPN-UHFFFAOYSA-N 0.000 description 7
- 125000005395 methacrylic acid group Chemical class 0.000 description 7
- 238000012545 processing Methods 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 6
- 229910001873 dinitrogen Inorganic materials 0.000 description 6
- 238000009826 distribution Methods 0.000 description 6
- 239000000523 sample Substances 0.000 description 6
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 5
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 230000003679 aging effect Effects 0.000 description 4
- 229910003460 diamond Inorganic materials 0.000 description 4
- 239000010432 diamond Substances 0.000 description 4
- 230000001747 exhibiting effect Effects 0.000 description 4
- 238000005187 foaming Methods 0.000 description 4
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical class CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 4
- 239000011261 inert gas Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 150000002978 peroxides Chemical class 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 230000000007 visual effect Effects 0.000 description 4
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 3
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- 229920000180 alkyd Polymers 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 238000002296 dynamic light scattering Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000010348 incorporation Methods 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 239000010690 paraffinic oil Substances 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 239000010734 process oil Substances 0.000 description 3
- 230000000153 supplemental effect Effects 0.000 description 3
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 3
- BWSZXUOMATYHHI-UHFFFAOYSA-N tert-butyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(C)(C)C BWSZXUOMATYHHI-UHFFFAOYSA-N 0.000 description 3
- 229920002554 vinyl polymer Chemical group 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- 238000004566 IR spectroscopy Methods 0.000 description 2
- 150000001253 acrylic acids Chemical class 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- 239000010692 aromatic oil Substances 0.000 description 2
- 239000010426 asphalt Substances 0.000 description 2
- 238000005102 attenuated total reflection Methods 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000011258 core-shell material Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000012933 diacyl peroxide Substances 0.000 description 2
- 239000004815 dispersion polymer Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000002689 maleic acids Chemical class 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000004611 spectroscopical analysis Methods 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- 238000012800 visualization Methods 0.000 description 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical group N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- XAAPVYJIDFCPRX-UHFFFAOYSA-N 4-hydroxyheptane-2,6-dione;prop-2-enamide Chemical compound NC(=O)C=C.CC(=O)CC(O)CC(C)=O XAAPVYJIDFCPRX-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004859 Copal Substances 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 241000782205 Guibourtia conjugata Species 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 150000004770 chalcogenides Chemical class 0.000 description 1
- UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- OWMBTIRJFMGPAC-UHFFFAOYSA-N dimethylamino 2-methylprop-2-enoate Chemical compound CN(C)OC(=O)C(C)=C OWMBTIRJFMGPAC-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 229940097789 heavy mineral oil Drugs 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 229940059904 light mineral oil Drugs 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 238000001507 sample dispersion Methods 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000002798 spectrophotometry method Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 238000002076 thermal analysis method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 238000004627 transmission electron microscopy Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/003—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
- C08F265/06—Polymerisation of acrylate or methacrylate esters on to polymers thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
- Y10T428/1379—Contains vapor or gas barrier, polymer derived from vinyl chloride or vinylidene chloride, or polymer containing a vinyl alcohol unit
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Laminated Bodies (AREA)
- Graft Or Block Polymers (AREA)
Abstract
Cette invention concerne des compositions de vernis de surimpression (OPV) contenant des dispersions essentiellement non aqueuses, de viscosité élevée qui comprennent des particules polymères acryliques de type cur/coque dans un solvant non aqueux tel qu'une huile minérale. Cette invention concerne également des procédés d'enduction d'un substrat avec un OPV à base desdites dispersions non aqueuses pour améliorer ses propriétés quand il est utilisé pour enduire un substrat, et obtenir une résistance au frottement, une résistance au jaunissement améliorées et des valeurs de brillant recherchées.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161568215P | 2011-12-08 | 2011-12-08 | |
| US61/568,215 | 2011-12-08 | ||
| PCT/US2012/068300 WO2013086231A1 (fr) | 2011-12-08 | 2012-12-06 | Vernis de surimpression à base de dispersions non aqueuses |
Publications (2)
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|---|---|
| CA2857192A1 CA2857192A1 (fr) | 2013-06-13 |
| CA2857192C true CA2857192C (fr) | 2020-04-28 |
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| CA2857192A Active CA2857192C (fr) | 2011-12-08 | 2012-12-06 | Vernis de surimpression a base de dispersions non aqueuses |
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| US (1) | US9988550B2 (fr) |
| EP (1) | EP2780424B1 (fr) |
| JP (1) | JP2015502433A (fr) |
| CN (1) | CN104093797A (fr) |
| CA (1) | CA2857192C (fr) |
| WO (1) | WO2013086231A1 (fr) |
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| JP6231890B2 (ja) * | 2014-01-16 | 2017-11-15 | 理想科学工業株式会社 | インク用後処理剤 |
| JP6663474B1 (ja) * | 2018-12-25 | 2020-03-11 | 日本ペイント・オートモーティブコーティングス株式会社 | クリヤー塗料組成物及びクリヤー塗膜の形成方法 |
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|---|---|---|---|---|
| US3985703A (en) | 1975-06-24 | 1976-10-12 | Rohm And Haas Company | Process for manufacture of acrylic core/shell polymers |
| US4264678A (en) | 1979-05-29 | 1981-04-28 | Gaf Corporation | Core-shell polymers |
| US4375532A (en) | 1980-11-03 | 1983-03-01 | Monsanto Company | Multiphase core/shell polymers |
| US4419471A (en) | 1981-09-04 | 1983-12-06 | Gaf Corporation | Core-shell polymers |
| US4469826A (en) | 1983-06-02 | 1984-09-04 | Sun Chemical Corporation | Process for the production of dispersions of polymers in non-aqueous vehicles |
| US4916171A (en) | 1984-07-25 | 1990-04-10 | Rohm And Haas Company | Polymers comprising alkali-insoluble core/alkali-soluble shell and copositions thereof |
| US4994524A (en) | 1985-12-13 | 1991-02-19 | Monsanto Company | Rubber modified reaction moldable nylon-6 compositions |
| US4888395A (en) | 1987-07-02 | 1989-12-19 | Mobil Oil Corporation | Core/shell polymers and improved sealable articles treated with the same |
| CA1335908C (fr) | 1988-10-07 | 1995-06-13 | Junji Oshima | Polymere ame/gaine, composes contenant les polymeres et articles moules |
| US5087663A (en) | 1989-03-08 | 1992-02-11 | The Dow Chemical Company | Molding compositions with methyl (meth)acrylate-butadiene-styrene graft copolymers |
| CA2027381A1 (fr) | 1989-10-14 | 1991-04-15 | Junji Oshima | Polymere pour trepans aleseurs, composition de resine d'articles moules faits avec ceux-ci |
| US5186993A (en) | 1991-10-11 | 1993-02-16 | Rohm And Haas Company | Polymer blends |
| BR9207043A (pt) * | 1991-12-24 | 1995-12-05 | Du Pont | Micropartículas duplamente estabilizadas e composição de revestimento |
| US5331025A (en) | 1992-11-04 | 1994-07-19 | Rohm And Haas Company | Coating compositions incorporating composite polymer particles |
| JP3664575B2 (ja) | 1997-08-19 | 2005-06-29 | 株式会社カネカ | メタクリル酸エステル系樹脂組成物及びそれを成形してなるフィルム |
| US6638995B1 (en) | 1998-11-30 | 2003-10-28 | Flint Ink Corporation | Printing inks |
| US6203973B1 (en) | 1999-03-25 | 2001-03-20 | Eastman Kodak Company | Polymer latexes with core-shell morphology |
| US6605404B2 (en) | 2001-09-28 | 2003-08-12 | Xerox Corporation | Coated Carriers |
| EP1371679B1 (fr) | 2002-06-14 | 2008-04-09 | Rohm And Haas Company | Composition aqueuse comprenant des nanoparticules polymériques |
| DE102004013637A1 (de) | 2004-03-19 | 2005-10-13 | Capsulution Nanoscience Ag | Verfahren zur Herstellung von CS-Partikeln und Mikrokapseln unter Verwendung poröser Template sowie CS-Partikel und Mikrokapseln |
| JP2005272563A (ja) * | 2004-03-24 | 2005-10-06 | Dainippon Ink & Chem Inc | オーバープリントニス |
| KR100603252B1 (ko) | 2004-04-29 | 2006-07-24 | 삼성전자주식회사 | 액체 토너 조성물 및 그 제조 방법 |
| AU2009260341B2 (en) | 2008-06-17 | 2014-09-18 | Sun Chemical Corporation | Fast setting sheet fed offset inks with non aqueous dispersion polymers |
| ES2531997T3 (es) * | 2009-07-30 | 2015-03-23 | Sun Chemical Corporation | Método para la reducción de olores en dispersiones no acuosas |
| ES2942566T3 (es) * | 2010-11-15 | 2023-06-02 | Sun Chemical Corp | Composiciones y métodos para mejorar las propiedades de fijación y resistencia al frotado de tintas de impresión |
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2012
- 2012-12-06 US US14/363,130 patent/US9988550B2/en active Active
- 2012-12-06 CA CA2857192A patent/CA2857192C/fr active Active
- 2012-12-06 CN CN201280066333.3A patent/CN104093797A/zh active Pending
- 2012-12-06 WO PCT/US2012/068300 patent/WO2013086231A1/fr active Application Filing
- 2012-12-06 EP EP12809428.1A patent/EP2780424B1/fr not_active Not-in-force
- 2012-12-06 JP JP2014546093A patent/JP2015502433A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| US9988550B2 (en) | 2018-06-05 |
| CA2857192A1 (fr) | 2013-06-13 |
| WO2013086231A1 (fr) | 2013-06-13 |
| JP2015502433A (ja) | 2015-01-22 |
| EP2780424A1 (fr) | 2014-09-24 |
| EP2780424B1 (fr) | 2015-10-28 |
| CN104093797A (zh) | 2014-10-08 |
| US20140370220A1 (en) | 2014-12-18 |
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Effective date: 20171116 |